Allele Registry

Canonical Allele Identifier: PA2826567569

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000588420

ClinVar Variation:

496049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Leu250Val	CA397836620 NM_001276761.3:c.748C>G